Quantification of Temperature-Dependent Sorption Kinetics in Shale Gas Reservoirs: Experiment and Theory

2021 ◽  
Author(s):  
Yun Yang ◽  
Shimin Liu

Abstract A critical component of natural gas in organic-rich shales is adsorbed gas within organic matter. Quantification of adsorbed gas is essential for reliable estimates of gas-in-place in shale reservoirs. However, conventional high-pressure adsorption measurements for coal on the volumetric method are prone to error when applied to characterize sorption kinetics in shale-gas systems due to limited adsorption capacity and finer pores of shale matrix. An innovated laboratory apparatus and measurement procedures have been developed for accurate determination of the relatively small amount of adsorbed gas in the Marcellus shale sample. The custom-built volumetric apparatus is a differential unit composed of two identical single-sided units (one blank and one adsorption side) connected with a differential pressure transducer. The scale of the differential pressure transducer is ± 50 psi, a hundred-fold smaller than the absolute pressure transducer measuring to 5000 psi, leading to a significant increase in the accuracy of adsorption measurement. Methane adsorption isotherms on Marcellus shale are measured at 303, 313, 323 and 333 K with pressure up to 3000 psi. A fugacity-based Dubinin-Astakhov (D-A) isotherm is implemented to correct for the non-ideality and predict the temperature-dependence of supercritical gas sorption. The Marcellus shale studied displays generally linear correlations between adsorption capacity and pressure over the range of temperature and pressure investigated, indicating the presence of a solute gas component. It is noted that the condensed phase gas storage exists as the adsorbed gas on shale surface and dissolved gas in kerogen, where the solute gas amount is proportional to the partial pressure of that gas above the solution. To our best understanding, it is the first time to observe the contribution of dissolved gas to total gas storage. With adsorption potential being modeled by a temperature dependence expression, the D-A isotherm can successfully describe supercritical gas sorption for shale at multiple temperatures. Adsorption capacity remarkably decreases with temperature attributed to the isosteric heat of adsorption. Lastly, the wide applicability of the proposed fugacity-based D-A model is also tested for literature adsorption data on Woodford, Barnett, and Devonian shale. Overall, the fugacity-based D-A isotherm provides precise representations of the temperature-dependent gas adsorption on shales investigated in this work. The application of the proposed adsorption model allows predicting adsorption data at multiple temperatures based on the adsorption data collected at a single temperature. This study lays the foundation for accurate evaluation of gas storage in shale.

2009 ◽  
Vol 6 (4) ◽  
pp. 1167-1175
Author(s):  
K. Srinivasan ◽  
E. Sathiya

The simultaneous adsorption of Pb(II) and Hg(II) on cottonseed carbon (CSC) was employed for the removal of these metals from wastewater. The influence of various factors such as agitation time, pH and carbon dosage on the adsorption capacity has been studied. Langmuir and Freundlich equation could be used to interpret adsorption data. Sorption kinetics has indicated that reversible first order kinetics model could be applied with film diffusion as the controlling mechanism.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shella Permatasari Santoso ◽  
Vania Bundjaja ◽  
Artik Elisa Angkawijaya ◽  
Chintya Gunarto ◽  
Alchris Woo Go ◽  
...  

AbstractNitrogen-grafting through the addition of glycine (Gly) was performed on a metal- phenolic network (MPN) of copper (Cu2+) and gallic acid (GA) to increase its adsorption capacity. Herein, we reported a one-step synthesis method of MPN, which was developed according to the metal–ligand complexation principle. The nitrogen grafted CuGA (Ng-CuGA) MPN was obtained by reacting Cu2+, GA, and Gly in an aqueous solution at a molar ratio of 1:1:1 and a pH of 8. Several physicochemical measurements, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), N2 sorption, X-ray diffraction (XRD), and thermal gravimetry analysis (TGA), were done on Ng-CuGA to elucidate its characteristics. The analysis revealed that the Ng-CuGA has non-uniform spherical shaped morphology with a pore volume of 0.56 cc/g, a pore size of 23.25 nm, and thermal stability up to 205 °C. The applicational potential of the Ng-CuGA was determined based on its adsorption capacity against methylene blue (MB). The Ng-CuGA was able to adsorb 190.81 mg MB per g adsorbent at a pH of 6 and temperature of 30 °C, which is 1.53 times higher than the non-grafted CuGA. Detailed assessment of Ng-CuGA adsorption properties revealed their pH- and temperature-dependent nature. The adsorption capacity and affinity were found to decrease at a higher temperature, demonstrating the exothermic adsorption behavior.


Minerals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 63
Author(s):  
Weidong Xie ◽  
Meng Wang ◽  
Hongyue Duan

Adsorbed gas is one of the crucial occurrences in shale gas reservoirs; thus, it is of great significance to ascertain the adsorption capacity of shale and the adsorption characteristics of CH4. In this investigation, the Taiyuan–Shanxi Formations’ coal-measure shale gas reservoir of the Carboniferous–Permian era in the Hedong Coalfield was treated as the research target. Our results exhibit that the shale samples were characterized by a high total organic carbon (TOC) and over to high-over maturity, with an average TOC of 2.45% and average Ro of 2.59%. The mineral composition was dominated by clay (62% on average) and quartz (22.45% on average), and clay was mainly composed of kaolinite and illite. The Langmuir model showed a perfect fitting degree to the experimental data: VL was in the range of 0.01 cm3/g to 0.77 cm3/g and PL was in the range of 0.23–8.58 MPa. In addition, the fitting degree depicted a linear negative correlation versus TOC, while mineral composition did not exhibit a significant effect on the fitting degree, which was caused by the complex pore structure of organic matter, and the applicability of the monolayer adsorption theory was lower than that of CH4 adsorption on the mineral’s pore surface. An apparent linear positive correlation of VL versus the TOC value was recorded; furthermore, the normalized VL increased with the growth of the total content of clay mineral (TCCM), decreased with the growth of the total content of brittle mineral (TCBM), while there was no obvious correlation of normalized VL versus kaolinite, illite and quartz content. The huge amount of micropores and complex internal structure led to organic matter possessing a strong adsorption capacity for CH4, and clay minerals also promoted adsorption due to the development of interlayer pores and intergranular pores.


2012 ◽  
Vol 550-553 ◽  
pp. 2259-2262
Author(s):  
Song Bo Cui ◽  
Hua Yong Zhang ◽  
Lu Yi Zhang

The adsorption behavior of methylene blue (MB) dye from aqueous solutions onto honeycomb-cinder (HC) and its acid-activated product was investigated in a batch system. The results showed the adsorption capacity was decreased for raw HC samples with the increase of pH value, while it was increased for activated samples. The adsorption data were fit with Langmuir isotherm model for MB adsorption by all samples. The MB adsorption capacity on samples was increased from 2.62 mg/g to 7.81 mg/g and 7.00 mg/g after acid-activated by HCl and H2SO4, respectively. The adsorption processes of MB followed pseudo-second-order kinetics with a coefficient of correlation≥0.99. This study demonstrated that acid-activated HC has superior adsorbing ability for MB than raw HC and can be used as alternative adsorbents in dye wastewater treatment.


SAINTIFIK ◽  
2020 ◽  
Vol 6 (2) ◽  
pp. 104-115
Author(s):  
Agusriyadin Agusriyadin

Penelitian ini bertujuan untuk menguji kemampuan AK dan AKPM dalam mengadsorpsi ion Cu (II), pengaruh parameter adsorpsi dan mekanisme adsorpsi. AK dan AKP Madsorben dibuat dari residu ampas kelapa. Adsorben dikarakterisasi dengan FTIR, SEM dan EDS. Pengaruh parameter adsorpsi seperti pH awal, dosis adsorben, waktu kontak dan konsentrasi ion Cu (II) awal diperiksa untuk menentukan kondisi optimum serapan tembaga (II). Ion Cu (II) yang teradsorpsi diukur berdasarkan pada konsentrasi Ion Cu (II) sebelum dan sesudah adsorpsi menggunakan metode AAS. Hasil karakterisasi menunjukkan bahwa struktur pori dan gugus fungsi tersedia pada permukaan adsorben. Menurut percobaan efek pH, kapasitas adsorpsi maksimum dicapai pada pH 7. Waktu kontak optimal dan konsentrasi tembaga awal (II) ditemukan masing-masing pada 120 menit dan 100 mg L-1. Data eksperimental sesuai dengan model kinetik orde dua orde dua, dan Langmuir isoterm adsorpsi yang diperoleh paling sesuai dengan data adsorpsi. Kapasitas adsorpsi maksimum adsorben ditemukan menjadi 4,73 dan 6,46 mg g-1 pada kondisi optimal. The results of characterization showed that the pore structure and the functional groups were available on adsorbent surface. According to the pH effect experiments, the maximum adsorption capacity was achieved at pH 7. Optimum contact time and initial copper(II) concentration were found at 120 min and 100 mg L-1, respectively. The experimental data were comply with the pseudo-second-order kinetic model, and Langmuir adsorption isotherm obtained best fitted the adsorption data. The maximum adsorption capacity of the adsorbents was found to be 4.73 and 6.46 mg g-1 at optimum conditions.


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